Spencer E Escobedo, Aashka Shah, Alyssa N Easton, Hana Hall, Vikki M Weake
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We compared several Gal4 drivers from the Bloomington <i>Drosophila</i> Stock Center (BDSC) including <i>GMR-Gal4, longGMR-Gal4</i> and <i>Rh1-Gal4</i> with newly developed Gal4 and QF2 drivers that are specific to different cell types in the adult eye. In addition, we generated drug-inducible <i>Rh1-GSGal4</i> lines and compared their induced expression with an available <i>GMR-GSGal4</i> line. Although both lines had significant induction of gene expression measured by luciferase activity, <i>Rh1-GSGal4</i> was expressed at levels below the detection of the fluorescent reporter by confocal microscopy, while <i>GMR-GSGal4</i> showed substantial reporter expression in the absence of drug by microscopy. Overall, our study systematically characterizes and compares a large toolkit of eye- and photoreceptor-specific drivers, while also uncovering some of the limitations of currently available expression systems in the adult eye.</p>","PeriodicalId":12128,"journal":{"name":"Fly","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/19336934.2021.1915683","citationCount":"6","resultStr":"{\"title\":\"Characterizing a gene expression toolkit for eye- and photoreceptor-specific expression in Drosophila.\",\"authors\":\"Spencer E Escobedo, Aashka Shah, Alyssa N Easton, Hana Hall, Vikki M Weake\",\"doi\":\"10.1080/19336934.2021.1915683\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Binary expression systems are a powerful tool for tissue- and cell-specific research. Many of the currently available <i>Drosophila</i> eye-specific drivers have not been systematically characterized for their expression level and cell-type specificity in the adult eye or during development. Here, we used a luciferase reporter to measure expression levels of different drivers in the adult <i>Drosophila</i> eye, and characterized the cell type-specificity of each driver using a fluorescent reporter in live 10-day-old adult males. We also further characterized the expression pattern of these drivers in various developmental stages. We compared several Gal4 drivers from the Bloomington <i>Drosophila</i> Stock Center (BDSC) including <i>GMR-Gal4, longGMR-Gal4</i> and <i>Rh1-Gal4</i> with newly developed Gal4 and QF2 drivers that are specific to different cell types in the adult eye. In addition, we generated drug-inducible <i>Rh1-GSGal4</i> lines and compared their induced expression with an available <i>GMR-GSGal4</i> line. Although both lines had significant induction of gene expression measured by luciferase activity, <i>Rh1-GSGal4</i> was expressed at levels below the detection of the fluorescent reporter by confocal microscopy, while <i>GMR-GSGal4</i> showed substantial reporter expression in the absence of drug by microscopy. 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Characterizing a gene expression toolkit for eye- and photoreceptor-specific expression in Drosophila.
Binary expression systems are a powerful tool for tissue- and cell-specific research. Many of the currently available Drosophila eye-specific drivers have not been systematically characterized for their expression level and cell-type specificity in the adult eye or during development. Here, we used a luciferase reporter to measure expression levels of different drivers in the adult Drosophila eye, and characterized the cell type-specificity of each driver using a fluorescent reporter in live 10-day-old adult males. We also further characterized the expression pattern of these drivers in various developmental stages. We compared several Gal4 drivers from the Bloomington Drosophila Stock Center (BDSC) including GMR-Gal4, longGMR-Gal4 and Rh1-Gal4 with newly developed Gal4 and QF2 drivers that are specific to different cell types in the adult eye. In addition, we generated drug-inducible Rh1-GSGal4 lines and compared their induced expression with an available GMR-GSGal4 line. Although both lines had significant induction of gene expression measured by luciferase activity, Rh1-GSGal4 was expressed at levels below the detection of the fluorescent reporter by confocal microscopy, while GMR-GSGal4 showed substantial reporter expression in the absence of drug by microscopy. Overall, our study systematically characterizes and compares a large toolkit of eye- and photoreceptor-specific drivers, while also uncovering some of the limitations of currently available expression systems in the adult eye.
期刊介绍:
Fly is the first international peer-reviewed journal to focus on Drosophila research. Fly covers a broad range of biological sub-disciplines, ranging from developmental biology and organogenesis to sensory neurobiology, circadian rhythm and learning and memory, to sex determination, evolutionary biology and speciation. We strive to become the “to go” resource for every researcher working with Drosophila by providing a forum where the specific interests of the Drosophila community can be discussed. With the advance of molecular technologies that enable researchers to manipulate genes and their functions in many other organisms, Fly is now also publishing papers that use other insect model systems used to investigate important biological questions.
Fly offers a variety of papers, including Original Research Articles, Methods and Technical Advances, Brief Communications, Reviews and Meeting Reports. In addition, Fly also features two unconventional types of contributions, Counterpoints and Extra View articles. Counterpoints are opinion pieces that critically discuss controversial papers questioning current paradigms, whether justified or not. Extra View articles, which generally are solicited by Fly editors, provide authors of important forthcoming papers published elsewhere an opportunity to expand on their original findings and discuss the broader impact of their discovery. Extra View authors are strongly encouraged to complement their published observations with additional data not included in the original paper or acquired subsequently.